MES Manager: Lead Digital Manufacturing & ERP Integrations

Accenture PLC

Chicago (IL)

Remote

USD 87,000 - 254,000

Full time

3 days ago
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Job summary

Accenture plc is seeking an ambitious Manufacturing Systems (MES) Manager to lead the design, development, and deployment of MES solutions across life sciences manufacturing environments. The role emphasizes close collaboration with business leaders to define needs, document configurations, and ensure validation per GxP standards.

Travel may be required based on client engagements. The ideal candidate brings at least 5 years of MES experience, strong FDA/GMP knowledge, and proven SDLC expertise

Qualifications

  • Minimum 5 years' MES experience in highly automated Life Sciences manufacturing.
  • Knowledge of FDA and GMP guidelines.
  • Strong written and oral communication; team collaboration.
  • Experience with SDLC and validation processes.
  • Bachelor's degree or equivalent work experience (12 years).

Responsibilities

  • Lead design, development, documentation, and implementation of MES.
  • Design/Author/Develop/Configure Electronic Batch Records (EBR).
  • Implement MES solutions and integrate with ERP and control equipment.
  • Documentation of MES configuration and validation of EBRs.
  • Collaborate with business management to define needs and design value-added solutions.
  • Document and analyze information needs per GxP standards.
  • Respond to client proposals and manage client relationships.

Skills

MES
GxP knowledge
SDLC
Team collaboration
Communication

Education

Bachelor's degree or equivalent

Tools

ERP systems

Job description

Accenture plc is seeking an ambitious Manufacturing Systems (MES) Manager to lead the design, development, and deployment of MES solutions across life sciences manufacturing environments. The role emphasizes close collaboration with business leaders to define needs, document configurations, and ensure validation per GxP standards.

Travel may be required based on client engagements. The ideal candidate brings at least 5 years of MES experience, strong FDA/GMP knowledge, and proven SDLC expertise

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